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United States Patent |
5,272,234
|
Chen
,   et al.
|
December 21, 1993
|
Photo-responsive conductive polymers and the processes of making the same
Abstract
Conjugated conductive polymers which are photo-responsive upon ultra-violet
light or visible light irradiation are prepared from copolymerization of
photo-responsive groups containing heterocyclic monomers and 3-substituted
heterocyclic monomers with the substituent containing a flexible segment
like an alkyl group, ethoxyl group or siloxane group. The conductivity of
the polymer can be controlled reversibly by irradiation of light and so
can be used in optical-electronic applications or a production of
detectors.
Inventors:
|
Chen; Show-An (Hsinchu, TW);
Liao; Chien-Hsiun (Feng Yuan, TW)
|
Assignee:
|
National Science Council (Taipei, TW)
|
Appl. No.:
|
867460 |
Filed:
|
April 13, 1992 |
Current U.S. Class: |
526/256; 257/E51.012; 257/E51.028; 526/258; 526/266; 526/279; 526/287; 526/297; 526/310; 526/313; 526/317.1 |
Intern'l Class: |
C08F 228/06; C08F 226/06; C08F 230/08; C08F 220/70 |
Field of Search: |
526/256
|
References Cited
U.S. Patent Documents
5204424 | Apr., 1993 | Roncali et al. | 526/256.
|
Primary Examiner: Schofer; Joseph L.
Assistant Examiner: Cheng; Wu C.
Attorney, Agent or Firm: Bednarek; Michael D.
Claims
We claim:
1. A photo-responsive conductive polymer which has a general formula of:
##STR20##
wherein X is selected from the group consisting of S, NH and O; R is
selected from the group consisting of --(CH.sub.2).sub.n --, --(CH.sub.2
--CH.sub.2 --O).sub.n --, --(Si-O).sub.n --, --(CH.sub.2).sub.n --O--,
##STR21##
wherein n is an integer from 1 to 12, Y is selected from the group
consisting of
##STR22##
R' is selected from the group consisting of --OCH.sub.3, --CN, --NO.sub.2,
--H, --OH, --SO.sub.3 M , alkyl and --COOM, wherein M is selected from the
group consisting of H, Li, Na, K, Rb, Cs and Fr;
R" is selected from the group consisting of --(CH2).sub.n --CH.sub.3,
--(CH.sub.2 --CH.sub.2 --O).sub.n --CH.sub.3, --(Si-O).sub.n --CH.sub.3,
wherein n is an integer from 3 to 21; and
.alpha.is 0.05 to 1;
wherein said polymers has a molecular weight of 10,000 to 1,000,000.
Description
BACKGROUND OF THE INVENTION
The present invention relates to a photo-responsive conductive polymer and
the processes of making the same, and particularly to a copolymerization
of the 3-substituted thiophene monomers containing photo-responsive group
with 3-substituted thiophene monomers.
Conventionally, the conductivity of a conjugated conductive polymer is
about 10.sup.-12 -10.sup.-9 s/cm before doping about 10.sup.O -10.sup.5
s/cm after doping. Most of the conductive polymers can not be dissolved in
organic solvents or melt-processed due to the rigid conjugated bond.
Therefore, the polymers should be introduced with flexible side chains
such as long alkyl groups to make the polymer soluble in organic solvents
and melt-processable. On the other hand, in order to control the
conductivity of the polymers by external stimulation, a photo-responsive
functional group should be introduced into the polymers.
However, there is no disclosure related to a conductive polymer with
photo-chemically induced property. In the related organic compound, only
the Japan National Industrial Chemistry Laboratory discloses the synthesis
of an azobenzene group containing 7,7,8,8-tetracyanoquinodimethane (TCNQ)
derivatives and the making of a Langmuir-Blodget film which can change its
conductivity when irradiated with ultra-violet light; the variation rang
is about 35 %. But the entire preparation process is so complicated.
Furthermore, the film has poor mechanical strength due to its low
molecular weight, and can be easily fractured.
SUMMARY OF THE INVENTION
It is therefore an object of the present invention to provide a
photo-responsive conductive polymer having the characteristics of
conductivity, photo-responsiveness and processability, and also soluble in
organic solvents such as chloroform.
In order to achieve the object stated above, the present invention uses an
azobenzene group which has the photo-responsive property to modify
3-substituted thiophene monomers. The photo-responsive 3-alkyl thiophene
derivatives thus obtained are copolymerized with 3-substituted thiophene
monomers with flexible side chain such as alkyl groups with carbon number
of or more than four. The copolymers are soluble in organic solvent such
as chloroform because of the presence of long alkyl group in the side
chain. Also, the copolymers can be processed by solution casting to
produce a flexible free- standing film. The azobenzene group, when
irradiated with ultra-violet or visible light, can generate photoexcited
hopping sites allowing an increase in electrical conductivity of the
copolymer. Thus the introduce of azobenzene group can be used to control
the conductivity of the copolymers upon irradiation of light. Since the
copolymers of the present invention can be easily processed, and the film
so produced has adequate mechanical properties and photo-responsive
property, the copolymers can be used in optical-electronic applications or
in the production of detectors.
DETAILED DESCRIPTION OF THE PRESENT INVENTION
The copolymer of the present invention which is produced from the
copolymerization of an azobenzene group containing 3-substituted alkyl
thiophene monomers and 3-alkyl thiophene monomers has the properties of
electrical conductivity, solubility, as well as melt-processability. The
most important property, however, is its responsiveness to ultra-violet
light and visible light, there from the conductivity of the polymers can
be controlled reversibly through ultra-violet light or visible light
stimulation. In addition to the azobenzene group, other photo-responsive
isomerization groups like 1,2-stilbene and 1,2-azomethine can also be used
in the present invention since they can generate photoexcited hopping
sites also by the light irradiation. According to the side chain effect on
the poly(3-alkyl thiophene), the conductivity and solubility of
polly(3-alkyl thiophene) with the carbon numbers 4 to 18 are quite similar
(J. Phys. Chem., 1987, 91, 6706).
The process for preparing the photo-responsive conductive copolymers of the
present invention is characterized by the synthesis of photo-responsive
groups containing heterocyclic derivative monomers and 3-substituted
heterocyclic derivative monomers with a flexible substituent like alkyl
group, ethoxyl group or siloxane group. The polymer thus prepared has the
structural formula of:
##STR1##
and the formulae of the monomers are:
##STR2##
where
X is S, NX or O;
R is --(CH.sub.2).sub.n --, --(CH.sub.2 --CH.sub.2 --O).sub.n --,
--(Si--O).sub.n --, --(CH2).sub.n --O--,
##STR3##
n is an integer from 1 to 12,
Y is
##STR4##
R'is --OCH.sub.3, --CN, --NO.sub.2, --H, --OH, --SO.sub.3 M , alkyl or
--COOM, wherein M is H, Li, Na, K, Rb, Cs or Fr;
R" is --(CH2).sub.n --CH.sub.3, --(CH.sub.2 --CH.sub.2 --O).sub.n
--CH.sub.3, --(Si-O).sub.n --CH.sub.3, wherein n is an integer from 3 to
21;
.alpha. is 0.05 to 1; and the polymer has a molecular weight of 10,000 to
1,000,000.
The monomers are placed in chloroform solvent under nitrogen flow at room
temperature, and FeCl.sub.3 or others transition metal halides like
AlBr.sub.3, AlCl.sub.3, MoCl.sub.5, WCl.sub.6, NbCl.sub.5, TaCl.sub.4,
TiCl.sub.4, SnCl.sub.4, BF.sub.3 or ZnCl.sub.2 are used as an oxidizing
agent in the oxidation copolymerization.
The general procedure for the synthesis of the azobenzene containing
3-substituted thiophene monomers is described as follows. The chemical
reaction formulae and reaction conditions are shown in example 1. The
monomer is prepared by reflux of 3-(6-bromohexyl) thiophene) and
4-hydroxy-4'-methoxyazobenzene with a mole ratio of 1:1 in high purity
acetone solution for two days at 60.degree. c, using potassium carbonate
and potassium iodide as catalysts; and then a solid is obtained. The solid
is dissolved in dichloromethane and then filtered by silica gel column,
after that, the solution is crystallized by ethanol to purify the
compound, and 3-{6-[4-(4'-methoxyphenylazo) phenyloxy] hexyl) thiophene is
obtained. The preparation of 3-(6-bromohexyl) thiophene refers to Angew.
Chem. Int. Ed. Engl., 1990, 29, 419, and the preparation of
4-hydroxy-4'-methoxyazobenzene refers to Collect. Czech. Chem. Commun.,
1969, 34, 2982. 3-hexylthiophene is prepared from couple reaction of
3-bromothiophene with the Grignard reagent hexylmagnesium bromide in the
presence of the catalyst bis(1,3-diphenyphosphinopropane) nickel chloride,
followed with a purification step by distillation at reduced pressure.
The synthesis procedure for the copolymers of the present invention is
described as follows. A mixture of 10-25% of azobenzene containing
3-substituted thiophene derivative and 3-alkyl thiophene is dissolved in
chloroform. Under a nitrogen stream, ferric chloride is added dropwisely
into the chloroform solution, then the solution is stirred for 1 day at
room temperature. The solution is poured into methanol and a precipitate
is obtained. The precipitate is placed in a Soxhlet extractor for
extraction with methanol and acetone successively for 1 day. After vacuum
drying, the product is dissolved in chloroform, and then poured into a
Teflon mold under a nitrogen stream at room temperature to produce a cast
film with a thickness of about 20 to 100 .mu.m. The film is stable in air
and can retain its photo-responsive characteristic in air at room
temperature.
This and other objectives of the invention as well as more complete
understanding thereof maybe obtainable from the following specific
examples with accompanying figure, wherein:
FIG. 1 is the structure of the testing device for measuring conductivity of
the photo-responsive conductive polymers;
FIG. 2 is the variation of conductivity of the polymers before and after
irradiation according to example 3;
FIG. 3 is the variation of conductivity of the polymers before and after
irradiation according to example 4; and
FIG. 4 is the variation of conductivity of the polymers before and after
irradiation according to example 5.
EXAMPLE 1:
The Preparation of the Azobenzene Group containing 3 alkyl thiophene
derivative monomers
Synthesis 1: 3-hexylthiophene
(ref: Tetrahedron, 1982,38, 3347)
0.125 mole of n-hexylbromide was dissolved in 40 ml of ethyl ether. Then,
10 ml of ethyl ether was added in drops and also 0.13 mole of magnesium
chip was added. The mixture was refluxed for 5 to 6 hours and the Grignard
agent was obtained. The Grignard reagent was added to a solution
consisting of 70 mg of NiDPPPCl.sub.2 and 0.106 mole of 3-bromo thiophene
in drops at 0.degree. c, then the mixture was refluxed for 12 to 15 hours.
After that, the mixture was hydrolyzed with 40 ml of 1 N hydrochloric acid
and 150 ml of ice water. Then, ethyl ether was used to extract the mixture
for a few times, and the mixture was washed with water until the solution
was neutral. The extract was dried by sodium sulfate to remove the
solvent. The product of 3-hexylthiophene was obtained with a yield of 65%
after distillation under reduced pressure.
Synthesis 2: 3-azobenzenealkyl thiophene derivatives
(The reaction steps are shown in table I)
(i) 4-(4'-methylphenoxy)hexyl bromide
(ref : J. Chem. Soc. 1958, 3303)
A solution of 62 g of methoxy phenol in 50 ml of methanol was added into a
solution of 33.75g of potassium hydroxide in 100 ml of methanol. The
resulting solution was added dropwisely and slowly into 1 mole of .alpha.,
-dibromohexane in 200 ml of acetone within 1 hour. After a reflux of the
mixture for 1 hour, the mixture was concentrated and then diluted with
water. The oil layer of the mixture was extracted with ethyl ether. Then,
the ethyl ether layer was filtered and the filtrate was extracted with
water. The solution was dried by calcium chloride, and
4-(4'-methoxyphenoxy) hexylbromide (compound 1, with a yield of 62% was
obtained by distillation under reduced pressure.
(ii) 3-.omega.-(4-methoxyphenoxy) hexyl] thiophene
Using the Grignard cross couple reaction procedure as in synthesis 1,
compound 1 and 3-bromothiophene were coupled to give
3-[-(4-methoxyphenoxy) hexyl]thiophene. Compound 2 was obtained after
recrystallization with methanol, and the yield was 45%.
(iii)3-(.omega.-bromoalkyl)thiophene (ref:Synthesis,1983,249)
0.12 moles of 48% hydrobromic acid and 0.198 moles of acetic anhydride were
mixed and added dropwisely into 0.02 moles of compound 2 under a nitrogen
stream. The mixture was refluxed for 20-25 hours at 100.degree. c, and
then diluted with water. After the mixture was extracted with ethyl ether,
the organic layer was extracted with saturated sodium hydrogen carbonate
aqueous solution until the filtrate was neutral. The organic layer was
dried with sodium sulfate, and then concentrated to remove the solvent and
added with a mixed solvent of n-hexane/ethyl ether. The solution was
filtered and the filtrate was transferred into a short silica-gel column
for an elution, using n-hexane as the elution solvent. After the
separation, the solvent was removed and 3-(-bromohexyl)thiophene was
obtained (compound 3, with a yield of 60%).
(iv) 4-hydroxyl-4'-methoxyazobenzene
(ref:Collect.Czech. Chem. Commun., 1969, 34, 2982)
0.1 moles of p-methoxy aniline was dissolved in 28 ml of concentrated
hydrochloric acid and 28 ml of water was added. Then 0.1 moles of sodium
nitrite was dissolved in 350 ml of water and the solution was dropped
slowly at 0-5.degree. c into the aforementioned solution. 10 g of phenol,
4 g of sodium hydroxide and 21 g of sodium carbonate were dissolved in 350
ml of water and then added dropwisely into the above cold mixed solution
at 0-5.degree. C. After 15 minutes, hydrochloric acid with a pH at 2-3 was
added and the precipitate was washed twice with 50 ml of water. Compound
4, 4-hydroxyl-4'-methoxyazobenzene, was obtained with a yield of 82% after
filtration and recrystallization with chloroform.
(iv') 4-(4'-hydroxylazobenzene) benzonitrile
(ref : Makromol. Chem., 1984, 185, 1327)
Diazonium salt was prepared from aminobenzonitrile and sodium nitrite by
using the method described in step (iv). The same amount of phenol and
sodium hydroxide were dissolved in 250 ml of water, the solution was then
added to the cold diazonium salt solution. The mixture was stirred for 1
hour at room temperature, and the precipitate was obtained by filtration
and washed with water. The precipitate was dissolved again in a volume
ratio of ethanol aqueous solution, and acidified by adding hydrochloric
acid dropwisely. The precipitate was filtered out and dried, the product
4-(4,-hydroxylazobenzene benzonitrile) was obtained (compound 4,) with a
yield of 78%.
(v) 3-(6-[4-(4'-methoxybenzoazo)phenoxy]hexyl}thiophene
(ref : Makromol. Chem., Rapid Commun., 1986, 7,389)
16 mg of potassium carbonate and small amount of potassium iodide were
added to 1.7 mmol of compound 3 and compound 4 (or compound 4'), and then
dissolved in 30 ml of dried acetone. The solution was under reflux for 2
days at 60.degree. c, and then was filtered and the solvent was
evaporated. The residue was again dissolved in dichloro methane. After the
solution was filtered by silica-gel followed by removal of solvent and
recrystallization with ethanol, the product thus obtained was
3-azobenzenehexyl thiophene derivatives (for compound 5, the yield was
61%, and for compound 5', it was 72%).
TABLE 1
______________________________________
##STR5##
##STR6##
##STR7##
##STR8##
##STR9##
##STR10##
##STR11##
##STR12##
##STR13##
##STR14##
##STR15##
##STR16##
##STR17##
##STR18##
##STR19##
______________________________________
The structural analysis and the physical properties of the compounds
mentioned in the example are summarized as below:
(1) 3-hexyl thiophene
Colorless liquid, boiling pt.=50-51 c /0.15 torr., .sup.1 H NMR (400 MHz,
CDCl.sub.3, TMS standard).delta.=0.81 (dd, 3H;H-6), 1.18-1.22 (m, 2H;H-5),
1.23-1.27 (m, 4H;H-3, 4), 1.53 (m, 2H;H-2), 2.54 (t, 2H;H-5), 6.83 (dd,
IH;H-2'), 6.84 (dd,lH;H-4'), 7.13 (dd, IH;H-5'), Mass M+=168.
(2) compound 5
Brown color powder, melting pt.=66 c, lH NMR (400 MHz, CDCl.sub.3, TMS
standard) .delta.=1.29-1.45 (m, 4H;H-3,4), 1.55 (m, 2H;H-5), 1.71 (m,
2H;H-2), 2.55(t, 2H;H-6), 3.77 (s, 3H; OCH.sub.3), 3.91 (t, 2H;H-1), 6.85
(dd, IH;H-2'), 6.88 (dd, IH;H-4'), 6.90 (d, 2H;H.sub.Ph), 6.91 (d,
2H;H.sub.Ph), 7.14(dd, IH;H-5'), 7.76 (d, 2H;H.sub.Ph), 7.77 (d,
2H;H.sub.Ph), Mass M.sup.+ =394.
(3) compound 5'
Orange powder, melting pt.=117 c, .sup.1 H NMR (400 MHz, CDCl.sub.3, TMS
standard) .delta.=1.32-1.53 (m, 4H;H-3,4), 1.61 (m,2H;H-5), 1.77(m,
2H;H-2), 2.59 (t, 2H;H-6), 3.98 (t, 2H;H-1), 6.87 (dd, IH;H-2'), 6.93(dd,
IH;H-4'), 6.95 (d, 2H;H.sub.Ph), 7.17 (dd, IH;H-5,), 7.72 (d,
2H;H.sub.Ph), 7.85 (d, 2H;H.sub.Ph), 7.88(d, 2H;L H.sub.Ph), Mass M.sup.+
=389.
EXAMPLE 2
The Preparation of the Polymers
A 250 ml three-necked flask was filled with 100 ml of chloroform solvent
and 0.4M ferric chloride as an oxidizing agent. Under a stream of nitrogen
gas, 20 ml of chloroform solution containing 0.01 M of compound 5 and 0.09
M of 3-hexyl thiophene were added dropwisely and slowly. Polymerization
was carried out by stirring the solution for 1 day at room temperature
under a stream of nitrogen gas. The polymer so obtained was precipitated
out in methanol, and then the precipitate was extracted with methanol and
acetone successively for 1 day to remove the residue of oxidizing agent
and oligomer. The precipitate was dissolved in chloroform. After
filtration, the filtrate was concentrated and then placed in a Teflon mold
to produce a cast film. The film was then dried in vacuum until constant
weight was obtained. The film thus prepared was a dark red free standing
film with metallic luster, Tg (the glass transition temperature) is
12.9.degree. C, Mw (weight average molecular weight) is 80,000 and Mw/Mn
is 4.3.
EXAMPLE 3
According to FIG. 1, the free-standing film (about 60 .mu.m in thickness)
obtained in example 2 was sandwiched in between the transparent conductive
glass 2 and copper electrode 3, and the exposure area was about 0.7
cm.sup.2, the conductive glass 2 and copper electrode 3 were connected
with a copper wire. A UV light of long wavelength (UVP BLAK-RAY 100 W,
360nm) irradiated through the transparent glass for 5 minutes, then in
dark for 5 minutes, and this step was repeated for three times. The
conductivity was measured and the result is shown in FIG. 2. As shown in
FIG. 2, the conductivity increased by about 18% under UV-irradiation and
decreased in the dark. The variation in conductivity was reversible.
Furthermore, the conductivity variations at the initial periods are very
sharp when the UV light was on and off.
It is to be noted that the increase in conductivity during the UV
irradiation is not due to the trans-cis isomerization, since an
irradiation with visible light also generated the same result as to be
revealed in example 5. Indeed, it can be attributed to a generation of
photoexcited hopping sites in the azobenzene moiety upon irradiation of UV
or visible light.
EXAMPLE 4
The device used was the same as in example 3, and the content, of
azobenzene derivatives in the copolymer was 25 mole % (Tg=34.5.degree. c,
Mw=100,000, Mw/Mn=3.6). The film was about 20 .mu.m thick and was flexible
and extensible but slightly stiffer than that in example 3. The variation
of conductivity is shown in FIG. 3 and the maximum increase in
conductivity is about 150%. Again, the conductivity variations at the
initial periods are very sharp when the UV light was on and off.
EXAMPLE 5
The photo-responsive conductive polymer prepared as the procedure of
example 2 (containing 25 mole % of compound 5', Tg=36.9.degree. C, weight
average molecular weight Mw=170,000, Mw/Mn=16) was cast into thin film
with the thickness about 60 .mu.m. The variations of conductivity upon UV
light (.lambda.=365 nm), visible light (.lambda.>400 nm) and white light
(from the source of 100 w Hg-lamp without filter), are shown in FIG. 4. It
is shown that upon the irradiation of UV light and visible light, the
conductivity increases by about 60% and 160% respectively. This example
clearly indicated that the increase in conductivity upon light irradiation
is not resulted from an isomerization of the azobenzene moiety, since no
isomerization occurs upon irradiation with visible light.
While the preferred embodiments has been described, variations thereto will
occur to those skilled in the art within the scope of the present
inventive concepts which are delineated by the following claims.
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